N2 Selectivity of a Series of

Sep 6, 2016 - Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Islamic Republic of Iran. §...
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The influence of the amide groups in the CO/N selectivity of a series of isoreticular, interpenetrated metal-organic frameworks Vahid Safarifard, Sabina Rodríguez-Hermida, Vincent Guillerm, Inhar Imaz, Mina Bigdeli, Alireza A. Tehrani, Jordi Juanhuix, Ali Morsali, Mirian E. Casco, Joaquin Silvestre-Albero, Enrique V Ramos-Fernandez, and Daniel Maspoch Cryst. Growth Des., Just Accepted Manuscript • DOI: 10.1021/acs.cgd.6b01054 • Publication Date (Web): 06 Sep 2016 Downloaded from http://pubs.acs.org on September 10, 2016

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Crystal Growth & Design

The influence of the amide groups in the CO2/N2 selectivity of a series of isoreticular, interpenetrated metal-organic frameworks Vahid Safarifard,†,‡ Sabina Rodríguez-Hermida,† Vincent Guillerm,† Inhar Imaz,† Mina Bigdeli,‡ Alireza A. Tehrani,‡ Jordi Juanhuix,§ Ali Morsali, ‡* Mirian E. Casco,┴ Joaquín Silvestre-Albero,┴ Enrique V. Ramos-Fernandez┴ and Daniel Maspoch†,#* †

Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and The Barcelona Institute of Science and Technology, Campus UAB, Bellaterra, 08193 Barcelona, Spain. ‡ Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Islamic Republic of Iran. § ALBA Synchrotron, 08290 Cerdanyola del Vallès, Barcelona, Spain. ┴ Laboratorio de Materiales Avanzados, Departamento de Química Inorgánica-Instituto Universitario de Materiales, Universidad de Alicante, Ctra. San Vicente-Alicante s/n, 03690 San Vicente de Raspeig, Spain. # ICREA, Pg. Lluís Companys 23, 08010 Barcelona, Spain. Metal-Organic Frameworks, Amide, Adsorption, Separation, Breakthrough

ABSTRACT: Here we report the use of a pillaring strategy for the design and synthesis of three novel amide-functionalized metalorganic frameworks (MOFs), TMUs-22/-23/-24, isoreticular to the recently reported imine-functionalized TMU-6 and TMU-21 MOFs. An extensive study of their CO2 sorption properties and selectivity for CO2 over N2, from single gas sorption isotherms to breakthrough measurements, revealed that not only the incorporation of amide groups but also their accessibility is crucial to obtain enhanced CO2 sorption and CO2/N2 selectivity. Therefore, the MOF with more accessible amide groups (TMU-24) shows a CO2/N2 selectivity value of ca. 10 (as revealed by breakthrough experiments), which is ca. 500 % and 700 % of the selectivity values observed for the other amide-containing (TMU-22 and TMU-23) and imine-containing (TMU-6 and TMU-21) MOFs.

INTRODUCTION Microporous metal−organic frameworks (MOFs), constructed from metal-based nodes and polytopic organic ligands, are a promising class of porous materials for carbon capture, separation and storage owing to their very high surface areas, tuneable pore sizes and shapes, and adjustable pore surface functionality.1-3 For these specific applications, it is widely accepted that certain chemical functionalities located at the pore surfaces of MOFs can increase their CO2 uptake and selectivity.4-10 Among these functionalities, CO2 has been found to bind at unsaturated metal centres via the electron rich terminal oxygen atom11-13. Also, CO2 can interact with electron rich Lewis basic groups via electron deficient carbon atom.14 For this purpose, most efforts have been made on the direct and post-synthetic functionalization of MOFs with amine groups.15-18 More recently, another approach based on the combined optimization of pore size and high charge density has anticipated very promising results.4, 19, 20 Besides the use of amine groups, the intrinsic characteristics of the amide groups make them also very attractive to establish cooperative intermolecular interactions with CO2.21 Amide groups possess two types of donor-acceptor affinity sites: the -NH moiety that can act as an electron acceptor (Lewis acid), and the -C=O group that can act as an electron donor (Lewis base); both allowing to establish NH···OCO and NC=O···CO2 interactions.22-24 In the last few years, the study of some amide-functionalized MOFs has confirmed their

potential for selectively adsorb CO2.5, 22, 24-30 For example, Chen, Wang et al. have reported that pores decorated with acylamide groups in the Cu(II)-based UTSA-48 MOF promote strong interactions with CO2 and high selectivity for CO2 over CH4.5 Recently, Wang et al. reported a 3-fold interpenetrated acylamide-MOF that shows higher selective adsorption of CO2 rather than other gases with a significant isosteric heat.31 Similarly, Zaworotko et al. found that the decoration of a rhttype MOF also with acylamide functions can significantly enhance the CO2 uptake and the selective adsorption of CO2 over N2 in comparison to PCN-61; an isoreticular analogue with acetylene moieties instead of amide groups.24 Remarkably, comparable trends of selectivity have also been observed in other MOFs decorated with acylamide25-28 and oxamide22 groups as well as in some recent porous covalent organic frameworks also containing acylamide groups.29, 30 Recent studies reported by us have shown that a series of porous interpenetrated MOFs can be designed by pillaring 2D layers, comprising Zn(II) ions and the V-shaped dicarboxylate ligand 4,4ʹ-oxybisbenzoic acid (H2oba), with linear dipyridylbased ligands (Fig. 1).32-34 Following this approach, we found that the pores of the synthesized MOFs can be easily functionalized with the two groups incorporated in the pillar ligands since the pores of these MOFs, which run perpendicular to the {Zn(oba)} layers, are also delimited by these ligands.29, 30, 35 For example, the use of the pillar ligands N,Nʹ-bis-(4-pyridylmethylene)-1,4-benzenediamine (bpmb) and its naphthalene analogue N,Nʹ-bis-(4-pyridylmethylene)-

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Figure 1. 2D layers formed by the association between Zn(II) ions and oba linkers are further pillared by amide/imine-functionalized dipyridyl-based ligands yielding to 3D-interpenetrated porous pcu-MOFs.

1,5-naphthalenediamine (bpmn) recently allowed the formation of two isoreticular 3-fold interpenetrated MOFs showing pores functionalized with imine groups [called TMU6 and TMU-21 (TMU = Tarbiat Modares University)].33, 34 Herein, inspired by this approach and the potential of the amide groups for enhancing the selectivity towards CO2, we report the synthesis of three newly acylamide-containing MOFs. The selected pillar ligands are N,Nʹ-bis(4-pyridinyl)terephthalamide (bpta), N,Nʹ-(1,4phenylene)diisonicotinamide (bpfb), and N,Nʹ-bis-(4pyridylformamide)-1,5-naphthalenediamine (bpfn), Figures 1 and S1, which lead to the assembly of: [Zn2(oba)2(bpta)]·(DMF)3 (TMU-22; where DMF is N,Ndimethylformamide); [Zn2(oba)2(bpfb)]·(DMF)5 (TMU-23), in which the acylamide group is inverted in comparison to TMU22; and [Zn2(oba)2(bpfn)]·(DMF)2 (TMU-24), in which the use of the naphthalene analogue also induces that the acylamide groups are more directed towards the pores than in

TMU-22 and TMU-23 (Figure 2). Importantly, the resulting 3-fold interpenetrated TMUs-22/-23/-24 are isoreticular to TMU-6 and TMU-21. The similarities (structure and stability) and differences (functional group and accessibility) of these MOFs allow studying the influence of the amide and the imine groups on their N2 and CO2 sorption properties as well as on their selective sorption of CO2 over N2. More specifically, this latter selectivity was evaluated by performing kinetics and breakthrough experiments for a CO2/N2 gas mixture.

EXPERIMENTAL SECTION Materials and Characterization The commercially available reagents were used without further purification. Ligands, TMU-6 and TMU-21, were synthesized following reported procedures.33,34 See Supporting Information and Figure S1 for synthetic details. Elemental analyses were collected on a CHNS Thermo Scientific Flash 2000 elemental analyser. Powder X-ray diffraction (PXRD)

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measurements were collected on a Philips X’pert diffractometer with monochromatic Cu-Kα radiation (λCu = 1.5406 Å). Thermogravimetric analysis (TGA) were carried out in a Perkin Elmer Pyris 1 under N2 atmosphere and heating rate of 10 °C/min. Fourier transform infra-red (FT-IR) spectra were recorded on a Bruker Tensor 27FTIR spectrometer equipped with a Golden Gate diamond attenuated total reflection (ATR) cell, in absorption mode at room temperature.

General synthesis of TMU-22, TMU-23 and TMU-24 A mixture of Zn(NO3)2.6H2O (0.297 g, 1 mmol), H2oba (0.258 g, 1 mmol), and the corresponding amide ligand (0.5 mmol) and DMF (50 mL) was sonicated until all solids were uniformly dispersed (≈ 3 minutes) and divided into 7 glass vials. The vials were heated at 120 °C for 3 days and then cooled to room temperature. Colourless (TMU-22) and redbrown (TMU-23 and TMU-24) crystals were obtained as pure phases, washed by DMF, and dried at room temperature. Data for TMU-22. Yield: 44 %. FT-IR (cm−1): 1691 (m), 1595 (vs), 1504 (s), 1395 (vs), 1331 (m), 1298 (m), 1238 (vs), 1160 (vs), 1098 (m), 777 (m), 659 (m), 524 (m). EA on solvent free sample: calcd. (%) for C46H30N4O12Zn2: C, 57.46; H, 3.15; N, 5.83; found: C, 57.50; H, 3.11; N, 5.74. Data for TMU-23. Yield: 36 %. FT-IR (cm−1): 1673 (vs), 1597 (vs), 1540 (m), 1510 (m), 1399 (vs), 1309 (m), 1220 (vs), 1159 (s), 1088 (m), 1067 (m), 1014 (m), 801 (m), 658 (m), 524 (m). EA on solvent free sample: calcd. (%) for C46H30N4O12Zn2: C, 57.46; H, 3.15; N, 5.83; found: C, 57.00; H, 3.10; N, 5.65. Data for TMU-24. Yield: 38 %. IR (cm−1): 1667 (vs), 1595 (vs), 1570 (m), 1505 (s), 1386 (vs), 1235(s), 1158 (vs), 1089 (m), 1065 (m), 1015 (m), 878 (m), 659 (m), 522 (m). EA on solvent free sample: calcd. (%) for C50H32N4O12Zn2: C, 59.37; H, 3.19; N, 5.54; found: C, 57.10; H, 3.12; N, 5.01. Crystallography Crystallographic data for TMU-22 and TMU-23 were collected at 100 K at XALOC beamline at ALBA synchrotron36 (λ = 0.79474 Å and 0.82653 Å, respectively). Data were indexed, integrated and scaled using the XDS37 and IMOSFLM38 programs. Absorption correction was not applied. SCXRD for TMU-24 was collected at 293 K on a Bruker AXS SMART Apex diffractometer using graphite monochromated Mo-Kα radiation (λ = 0.71073 Å) and were corrected for Lorentz and polarization effects. The frames were integrated with the Bruker SAINT39 software package. Absorption corrections were applied using the program SADABS40 giving max./min. transmission factors of 1.000/0.270. The structures were solved by direct methods and subsequently refined by correction of F2 against all reflections, using SHELXS201341 and SHELXL201342 within the WinGX package.43 All non-hydrogen atoms were refined with anisotropic thermal parameters by full-matrix least-squares calculations on F2 using the program SHELXL2013. Hydrogen atoms were inserted at calculated positions and constrained with isotropic thermal parameters. In TMU-24,

the carbonyl group of the N,N-ligand is distorted in two positions with 55 % and 45 % of occupancy. The structures contain some disorder molecules. Attempts to adequately model of disordered DMF molecules (40 electrons) were unsatisfactory; therefore the PLATON/SQUEEZE44 routine has been applied to mask out the disordered electron density. The residual electron density was assigned to 3, 5 and 1 molecules of DMF in TMU-22 (509 electrons per unit cell), TMU-23 (876 electrons located per unit cell) and in TMU-24 (384 electrons per unit cell). Crystallographic and refinement data, and the main bond distances and angles are listed in Table 1 and Tables S1-3.

Table 1. Crystal and structure refinement data. Compound

TMU-22

TMU-23

TMU-24

Emp. formula

C55H51N7O15Z n2

C61H65N9O17Z n2

C28H23N3O7 Zn

Formula weight

1180.76

1326.96

578.86

Crystal system

Monoclinic

Monoclinic

Monoclinic

Space group

P21/n

P21/c

C2/c

CCDC ref.

1480227

1480228

1480229

Unit cell dimensions a (Å)

14.680(4)

15.110(3)

14.881(4)

b (Å)

24.780(5)

24.110(5)

24.993(6)

c (Å)

16.270(5)

15.910(5)

16.013(4)

β (deg)

113.27(5)

112.10(6)

111.422(5)

V (Å )

5437.0(2)

5370.2(2)

5544.0(2)

Z

4

4

8

F (000)

2440

2760

2384

θ range (°)

1.850-33.822

1.626-33.681

1.63028.396

Ind. Refln. (Rint)

11071 (0.1528)

12947 (0.1164)

6462 (0.0637)

Goodnessof-fit on F2

1.331

1.090

1.018

Final R indices [I > 2σ(I)]

R1 = 0.1402 wR2 = 0.3805

R1 = 0.0939 wR2 = 0.2444

R1 = 0.0717 wR2 = 0.1819

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Low-Pressure Sorption Measurements Volumetric N2 and CO2 sorption isotherms were collected at 77 K (N2) and 203 K, 258 K, 273 K, 288 K and 298 K (CO2) using an ASAP 2020 HD (Micromeritics). Temperature was controlled by using a liquid nitrogen bath (77 K) or a Lauda Proline RP 890 chiller (203 K – 298 K). The total pore volumes (Vt) were calculated at P/P0 = 0.95 (N2) and at 760 torr (CO2).

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Kinetics of adsorption Kinetic evaluation of the sorbents was performed at 298 K in a home-made glass manometric adsorption equipment using pure gas components (CO2 and N2). This equipment is constituted by a manifold of a well-known volume (to define the initial gas dose), a sample holder containing the adsorbent and a pressure transducer. Prior to the adsorption experiment, the samples were degassed under vacuum at the activation temperature used for single gas sorption experiments. The initial pressure in the manifold was defined at 500 mbar for all adsorbates. Once equilibrated, the manifold was expanded to the sample holder, pressure readings being recorded every second and lasting for ten minutes. Moreover, the sample holder was immersed in a temperature-controlled water bath at 298 K to minimize any heat effect due to the adsorption process itself. Breakthrough measurements Breakthrough curve experiments for different mixture of gases were carried out using a column. The samples powders were packed in the middle part of the column. Here, the samples masses used were 0.30 g. The flow rates of all gases were controlled by mass flow controllers. Before the measurement, the samples were activated at the desired temperature for 2 h using a He total flow of 50 mL.min-1. The gas stream from the outlet of the column was analysed online with a mass spectrometer. The CO2/N2 selectivities (σ) of samples were evaluated by the following equation:

 qCO2     pCO  2  σ =  q N2     pN   2 where qi is the adsorption capacity of i component, pi is the partial pressure of i component. The amount adsorbed for each gas was calculated by the integration of the breakthrough curves. For this purpose, breakthrough experiments with H2 (not adsorbed in these materials), have been performed using the same bed and the same flows. Then, the H2 breakthrough curve has been used to calculate the time zero and more importantly to consider the shape of the breakthrough in the integration. The amount of gas adsorbed was the different between the shape of the CO2 or N2 breakthrough and the H2 breakthrough. Thus, the dispersion and the very small pressure drop can be considered.

Results and discussion Synthesis and crystal structures TMUs-22/-23/-24 were synthesized following the same pillaring strategy reported for TMU-6 and TMU-21.33,34 Solvothermal reactions between Zn(NO3)2.6H2O, H2oba and the correspondent pillar ligand in DMF at 120 oC for 3 days produced prismatic crystals of TMUs-22/-23/-24 suitable for

Figure 2. View of the pore channels of a) TMU-6, b) TMU-22, c) TMU-23, d) TMU-21 and e) TMU-24, highlighting the acylamide groups. Colour code: N (green), O (purple), the more accessible O atoms in TMU-24 (lavender).

single-crystal X-ray diffraction analyses. The simulated (derived from the single crystal structures) and experimental powder X-ray diffraction (PXRD) patterns were consistent (Figure S2), confirming that all synthesized MOFs can be obtained as pure phases; as also corroborated by Fourier transformed infrared spectroscopy and elemental analysis (performed on the activated samples, vide infra). TMU-22 and TMU-23 crystallize in the monoclinic P21/n and P21/c space groups, respectively (Table 1). They are neutral 3-fold interpenetrated MOFs formed by {Zn(oba)} layers connected through the N,Nʹ-pillar ligands. As in TMU6, their basic unit is a dinuclear zinc cluster, in which both Zn(II) centres are penta-coordinated to four carboxylate O atoms from three fully deprotonated oba ligands and to one N atom from the N,Nʹ-donor ligand (Figure 1). The geometry around the metal centres can be described as a distorted square pyramid, with Addison parameter45 τ values in the range of

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0.35-0.49. In these structures, each nonlinear dicarboxylate oba ligand is coordinated to three Zn(II) centres forming the {Zn(oba)} layers along the ab plane. Because of the dinuclear nature of the metal cluster, these layers are formed by two sheets of parallel oba ligands that form π-π stacking interactions between them (Figure 1; Tables S4, S5). These {Zn(oba)} layers are then pillared by the linear acylamidefunctionalized ligands, extending the structure in three dimensions. It is important to mention here that, due to the conformational flexibility of both oba and bpta ligands, TMU22 is a supramolecular conformational isomer of a reported MOF.31 Although both compounds are 3-fold interpenetrated, they still possess apparent 1D pore channels (≈ 7.0 × 6.5 Å and ≈ 6.8 × 6.4 Å -including van der Waals (vdW) radii- for TMU-22 and TMU-23, respectively) running along the direction and noticeable free space (33 % for TMU-22 and 32 % for TMU-23), comparable to the values found for TMU-6 (≈ 8.1 × 7.4 Å; and 33 % free space)46 (Figures 1 and S3-5). The channels are filled with disordered guest solvent molecules, squeezed due to thermal disorder. TMU-24 crystallizes in the monoclinic C2/c space group (Table 1), showing a crystal structure isoreticular to those of TMUs-6/-21/-22/-23. Thus, it also consists on a 3-fold interpenetrated network that exhibits 1D pore channels of ≈ 6.7 × 5.5 Å (free space = 30 %) functionalized with acylamide groups. These values are similar to those exhibited by its imine-functionalized TMU-21 analogue, which shows a pore size of ≈ 8.2 × 7.0 Å and a free space of 30 %.46 (Figures S67). Here it is very important to note that, even though TMUs22/-23/-24 are isoreticular, their acylamide groups do not show the same orientation on the pore surfaces (Figure 2b,c,e) as well as do not participate in the same number of supramolecular interactions between the interpenetrated networks (Tables S4-6). In TMU-23, all donor –N-H and acceptor –C=O groups of the two acylamide groups per pillar ligand establish H-bonds and N-H···π interactions with the other two networks forming the 3-fold interpenetrated structure. In TMU-22, each donor –NH moiety of the two acylamide groups per pillar ligand establishes H-bonds with carboxylate groups of the other networks, whereas the two acceptor -C=O groups do not participate in H-bonds. In TMU24, only one of the two acylamide groups forms H-bonds. Interestingly, the other acylamide group is pointing towards the pores so that it does not participate in direct H-bonds with the other networks (Figure 2e). Altogether makes this acylamide group easily accessible to potential interactions with CO2 guest molecules. Contrariwise, even though all the other H-bonded acylamide groups of TMUs-22/-23/-24 are located on the surfaces of the pores, they are not directly pointing towards the channels, and therefore they are in principle less accessible to guest molecules.

Topology Topological analysis performed with TOPOS47 revealed that all the studied MOFs show the same 3-fold interpenetrated, 6connected net with pcu topology (Figure 1). The pcu topology is ubiquitous in MOFs, including the iconic MOF-5.48 Here, it is worth to mention that the pcu net is edge-transitive with cubic symmetry and Pm-3m space group. However, in the

present case, the overall symmetry of TMUs-22/-23/-24 decreased to monoclinic (Table 1). This symmetry decrease is attributed to the fact that the points of extension of the Zn(II) dimer do not match with the vertices of the perfect octahedron required to produce highly symmetrical pcu-MOFs (Figure 1). In addition, the use of a pillaring strategy with mixed ligands (including the flexible oba and pillar N,Nʹ-ligands) also forces the symmetry to differ from that of MOF-5.

Thermal stability The TGA diagrams of all as-synthesized materials revealed a first weight loss of 16.08 % (room temperature (r.t.)-300 °C) for TMU-6, 13.71 % (80-325 °C) for TMU-21, 9.93 % (100240 °C) for TMU-22, 15.16 % (r.t.-300 °C) for TMU-23, and 15.46 % (r.t.-325 °C) for TMU-24. In all cases, this weight loss was attributed to the removal of all guest solvent molecules. Decomposition of all materials starts at around 400 o C, confirming their high thermal stability (Figure S8). Activation process All compounds were activated using a very similar protocol that started with a solvent-exchange step. TMUs-6/-21 and TMUs-22/-23/-24 were immersed in acetonitrile and dichloromethane, respectively, for 3 days, during which the solvent was exchanged once daily. Note here that previous stability tests showed that all synthesized MOFs were stable in these solvents (Figure S9) for at least 24 h at r.t. Then, each MOF was evacuated for 12 h under vacuum at 150 °C prior to gas sorption measurements. It is noteworthy that PXRD diagrams collected after the sorption studies confirm that the frameworks retain their crystallinity and remained unaltered after both processes (Figure S10). These observations were further corroborated by elemental analysis and TGA, in which only the weight loses around 400 oC corresponding to their decomposition were observed (Figure S8). Nitrogen sorption at 77 K N2 isotherm at 77 K on TMU-22 showed a characteristic type I behaviour of microporous materials, as expected from its crystal structure (BET area (ABET) = 680 m2.g-1; pore volume (Vt) = 0.28 cm3.g-1). Contrariwise, TMU-21, TMU-23 and TMU-24 were found to be non-porous materials (negligible N2 uptake). In the case of TMU-6, it showed much lower porosity than that expected from its crystal structure (ABET = 150 m2.g-1; Vt = 0.08 cm3.g-1) (Table 2, Figure S11). Thus, all activated compounds, except TMU-22, reveal a “N2phobic” behavior.49-52 We reasoned that this behaviour could be due to the existence of different structural rearrangements depending on the MOF during sorption or when exposed to cryogenic temperatures and/or under vacuum, reducing/preventing access to the porosity. Indeed, similar temperature dependent behaviours are already well-known in soft materials such as in MIL-53 (Al).53 However, other factors cannot be fully excluded, such as the existence of strong interactions between N2 and the channel walls at 77 K that hinder diffusion into the material.54

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Crystal Growth & Design Table 2. Summary of BET areas, total pore volumes and CO2 uptakes observed for TMUs-6/-21-24. ABET (m2.g-1) (N2, 77 K)

Total Vt (cm3.g-1) (N2a / CO2b)

Theo Vt (cm3.g1 c )

TMU-6

150

0.08 / 0.32

0.22

9.0

TMU-21

≈0

≈ 0 / 0.16

0.25

4.5

TMU-22

680

0.28 / 0.25

0.25

7.2

TMU-23

≈0

≈ 0 / 0.27

0.27

7.2

TMU-24

≈0

≈ 0 / 0.22

0.25

6.3

a

calculated at P/P0 = 0.95. Calculated with PLATON.

b

CO2 uptakeb (mmol.g-1) (203 K)

Calculated at P = 760 torr.

30

-1

CO2 adsorption Qst (kJ.mol )

MOF

a

c

25 20 15 10 TMU-6 TMU-21 TMU-22 TMU-23 TMU-24

5 0 0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

1.6

700

800

-1

CO2 Loading (mmol.g )

b

2.0

-1

CO2 sorption at various temperatures and heats of adsorption Contrariwise to the adsorption of N2, the CO2 sorption isotherms at various temperatures revealed that all of them are porous (Figures 3a and S12a-16a). CO2 uptake at 203 K were calculated to be 9.0 mmol.g-1, 4.5 mmol.g-1, 7.2 mmol.g-1, 7.2 mmol.g-1 and 6.3 mmol.g-1 for TMU-6, TMU-21, TMU-22, TMU-23 and TMU-24, respectively (Table 2). The observed pore volumes (at 760 torr) were: 0.32 cm3.g-1 (TMU-6), 0.16 cm3.g-1 (TMU-21), 0.25 cm3 g-1 (TMU-22), 0.27 cm3.g-1 (TMU-23) and 0.22 cm3.g-1 (TMU-24). These pore volumes calculated from the CO2 adsorption data are in agreement with the theoretical values extracted from the crystal structures. The variations observed can be attributed to small structural changes widely observed in such interpenetrated sorbents.35, 55-

CO2 Uptake (mmol.g )

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

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Ads. TMU-6 TMU-21 TMU-22 TMU-23 TMU-24

1.5

1.0

0.5

0.0 0

100

200

300

400

500

600

Pressure (Torr)

57

Figure 3. (a) Heats of adsorption of CO2 and (b) CO2 sorption isotherms at 298 K for TMUs-6/-21-24.

Isosteric heats of adsorption of CO2 (Qst) were calculated from the isotherms collected at different temperatures (Table 2 and Figures S12-16). The two acylamide-functionalized TMU-24 and TMU-22 exhibited the highest Qst for CO2, from 24 to 26 kJ·mol-1 and 23 to 24 kJ·mol-1, respectively. The different Qst for CO2 between TMU-24, TMU-22, and TMU23 can be attributable to the different accessibility of their acylamide groups and to the different number of supramolecular interactions in which they are involved (vide supra).

CO2/N2 separation properties In light of the porosity of the materials for CO2 and their apparent low affinity for N2, we further investigated their potential for CO2/N2 separation by performing kinetics experiments (Figures 4 and S17). As expected, the highest selectivity (σ) for CO2 over N2 was observed for TMU-24 (σ = 14.1, Table 3); which is the material exhibiting the highest Qst of CO2 and with the most accessible acylamide groups pointing towards the porous channels. Overall, the CO2/N2 selectivity of TMU-24 estimated from kinetics experiment is ca. 70 % higher than for the other materials of the family.

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Table 3 Summary of CO2 separation properties in TMUs6/-21/-22/-23/-24. MOF

Qst of CO2 (kJ.mol-1)

17-14

TMU-6

Selectivity (Kinetics)

Selectivity (Breakthroug h, CO2:N2 1:1)

8.2

18-20

8.2

1.4

TMU-22

23-24

8.6

2.0

TMU-23

12-18

8.2

1.7

TMU-24

24-26

14.1

10.0

0.005

N2

CO2:N2 1:1

CO2

0.004

0.003

0.002

0.001

0.000 0

50

100

150

200

250

300

time (s)

b

0.020

N2

CO2:N2 1:9

CO2

0.015

0.010

0.005

0.000 0

1.8

TMU-21

a

mmol N2or CO2/s

These results were further confirmed by breakthrough experiments with CO2/N2 gas mixture (Figures 5 and S18). Once again, TMU-24 performed much better than its isoreticular variants, with a CO2/N2 selectivity of 10.0 at r.t. for an equimolar CO2/N2 gas mixture (Figure 5). This value represents 700 % of the selectivity found in similar conditions for its imine analogue TMU-21 (σ = 1.4). It also performs better than TMU-22 and TMU-23, the other acylamide containing MOFs with less accessible functional groups. Indeed, the selectivity of TMU-24 is 500 % and 580 % the selectivity of TMU-22 and TMU-23, respectively. Therefore, not only the incorporation of amide functional groups in the frameworks but also their accessibility for the CO2 guest molecules is crucial to enhance the CO2/N2 selectivity. This observation was further confirmed in more realistic gas mixture conditions (CO2:N2 = 1:9), in which TMU-24 was still found to perform well with a selectivity of 4.6 (Figure 5). It is important to remark that the CO2 adsorption capacity found in the breakthrough experiment at r.t. (≈ 0.65 mmol.g-1) for TMU-24 is slightly lower than the one extracted from the isotherm at 500 mbar and r.t. (≈ 0.85 mmol.g-1). This feature can be attributed to a small amount of N2 adsorbed in these conditions (298 K and gas mixture).

30

60

90

120

150

time (s)

Figure 5. CO2/N2 Breakthrough separation curves at 298 K for TMU-24 with total flow of 5 mL.min-1 for CO2:N2 = 1:1 (a) and 25 mL.min-1 for 1:9 (b).

CONCLUSIONS 0.8

CO2 N2

0.7

-1

Adsorbed amount (mmol.g )

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

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mmol N2 or CO2/s

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0.6 0.5 0.4 0.3 0.2 0.1 0.0 0

100

200

300

400

time (s)

Figure 4. Adsorption kinetics of CO2 and N2 for TMU-24 at 298 K (initial manifold pressure 500 mbar).

We successfully synthesized three novel, 3-fold interpenetrated pcu-MOFs containing acylamide functional groups (TMU-22, TMU-23 and TMU-24), isoreticular to the recently reported imine-containing MOFs, TMU-6 and TMU21. The study of their sorption properties revealed that the insertion of amide functional groups in MOFs does not necessarily induce a noticeable improvement of the CO2/N2 separation properties. Indeed, another aspect that needs to be addressed is the accessibility of the functional groups, especially in interpenetrated frameworks. If neglected, it could jeopardize the efficiency of MOFs functionalization, as illustrated by the performance of TMU-22 and TMU-23, two acylamide-functionalized analogues of the parent iminefunctionalized TMU-6; that all these three MOFs show negligible difference of the selectivity. This demonstrates the needs for smart materials design approaches, further confirmed by the deliberate alteration of the pore shape of TMU-24 using a bulky, central naphthalene core. This resulted in better accessibility of the acylamide groups,

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leading into a 70 % improvement of CO2/N2 selectivity according to kinetics studies (from 8.2 to 14.1 for TMU-21 and TMU-24, respectively). Moreover, a dramatic increase of the selectivity was obtained from breakthrough experiments. The CO2/N2 selectivity for TMU-24 corresponds to ca. 700 % of this imine- containing analogue, TMU-21. Moreover, its selectivity is ca. 500 % and 580 % of TMU-22 and TMU-23, two isoreticular, amide containing MOFs with less accessible functional groups.

ASSOCIATED CONTENT Supporting Information. Synthetic procedure for ligand synthesis, crystallographic data, PXRD diagrams, TGA plots, gas sorption and separation data. This material is available free of charge via the Internet at http://pubs.acs.org.

AUTHOR INFORMATION Corresponding Authors * E-mails: [email protected], [email protected]

Author Contributions The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript.

Notes The authors declare no competing financial interest.

ACKNOWLEDGMENTS This work was supported by the MINECO-Spain through projects PN MAT2015-65354-C2-1-R, 2014-SGR-80, MAT2013-45008-P and EU FP7 ERC-Co 615954. I.I. and E.V.R.F. thank the MINECO for the RyC fellowship RYC-2010-06530 and RyC2012-11427 and V.G. is grateful to the Generalitat de Catalunya for a Beatriu de Pinós Fellowship. ICN2 acknowledges the support of the Spanish MINECO through the Severo Ochoa Centers of Excellence Program, under Grant SEV-2013-0295. E.V.R.F. and J.S.A. acknowledge the Generalitat Valenciana for PROMETEOII/2014/004. Support of this investigation by Tarbiat Modares University is gratefully acknowledged.

REFERENCES (1) Zhou, H. C.; Long, J. R.; Yaghi (Eds.), O. M., Themed issue: Metal-Organic Frameworks, Chem. Rev., 2012, 112, 673-1268 (2) Long, J. R.; Yaghi (Eds.), O. M., Themed issue: MetalOrganic Frameworks, Chem. Soc. Rev., 2009, 38, 1201-1508 (3) Zhou, H. C.; Kitagawa (Eds.), S., Themed issue: MetalOrganic Frameworks, Chem. Soc. Rev., 2014, 43, 5415-6172 (4) Belmabkhout, Y.; Guillerm, V.; Eddaoudi, M., Chem. Eng. J. 2016, 296, 386-397. (5) Xiong, S.; He, Y.; Krishna, R.; Chen, B.; Wang, Z., Cryst. Growth Des. 2013, 13, 2670-2674. (6) Sumida, K.; Rogow, D. L.; Mason, J. A.; McDonald, T. M.; Bloch, E. D.; Herm, Z. R.; Bae, T.-H.; Long, J. R., Chem. Rev. 2012, 112, 724-781. (7) Liu, J.; Thallapally, P. K.; McGrail, B. P.; Brown, D. R.; Liu, J., Chem. Soc. Rev. 2012, 41, 2308-2322. (8) Vaidhyanathan, R.; Iremonger, S. S.; Shimizu, G. K.; Boyd, P. G.; Alavi, S.; Woo, T. K., Science 2010, 330, 650-653. (9) Li, B.; Zhang, Z.; Li, Y.; Yao, K.; Zhu, Y.; Deng, Z.; Yang, F.; Zhou, X.; Li, G.; Wu, H., Angew. Chem. Int. Ed. 2012, 51, 1412-1415.

Page 8 of 10

(10) Panda, T.; Pachfule, P.; Banerjee, R., Chem. Commun. 2011, 47, 7674-7676. (11) Caskey, S. R.; Wong-Foy, A. G.; Matzger, A. J., J. Am. Chem. Soc. 2008, 130, 10870-10871. (12) Zhang, S.-Y.; Zhang, X.; Li, H.; Niu, Z.; Shi, W.; Cheng, P., Inorg. Chem. 2015, 54, 2310-2314. (13) Llewellyn, P. L.; Bourrelly, S.; Serre, C.; Vimont, A.; Daturi, M.; Hamon, L.; De Weireld, G.; Chang, J.-S.; Hong, D.-Y.; Kyu Hwang, Y.; Hwa Jhung, S.; Férey, G., Langmuir 2008, 24, 72457250. (14) Chen, D.-M.; Xu, N.; Qiu, X.-H.; Cheng, P., Cryst. Growth Des. 2015, 15, 961-965. (15) McDonald, T. M.; Mason, J. A.; Kong, X.; Bloch, E. D.; Gygi, D.; Dani, A.; Crocella, V.; Giordanino, F.; Odoh, S. O.; Drisdell, W. S.; Vlaisavljevich, B.; Dzubak, A. L.; Poloni, R.; Schnell, S. K.; Planas, N.; Lee, K.; Pascal, T.; Wan, L. F.; Prendergast, D.; Neaton, J. B.; Smit, B.; Kortright, J. B.; Gagliardi, L.; Bordiga, S.; Reimer, J. A.; Long, J. R., Nature 2015, 519, 303-308. (16) Couck, S.; Denayer, J. F.; Baron, G. V.; Rémy, T.; Gascon, J.; Kapteijn, F., J. Am. Chem. Soc. 2009, 131, 6326-6327. (17) Demessence, A.; D'Alessandro, D. M.; Foo, M. L.; Long, J. R., J. Am. Chem. Soc. 2009, 131, 8784-8785. (18) Fracaroli, A. M.; Furukawa, H.; Suzuki, M.; Dodd, M.; Okajima, S.; Gándara, F.; Reimer, J. A.; Yaghi, O. M., J. Am. Chem. Soc. 2014, 136, 8863-8866. (19) Nugent, P.; Belmabkhout, Y.; Burd, S. D.; Cairns, A. J.; Luebke, R.; Forrest, K.; Pham, T.; Ma, S.; Space, B.; Wojtas, L.; Eddaoudi, M.; Zaworotko, M. J., Nature 2013, 495, 80-84. (20) Shekhah, O.; Belmabkhout, Y.; Chen, Z.; Guillerm, V.; Cairns, A.; Adil, K.; Eddaoudi, M., Nature Commun. 2014, 5, 4228. (21) de Lange, K. M.; Lane, J. R., J. Chem. Phys. 2011, 135, 064304. (22) Alsmail, N. H.; Suyetin, M.; Yan, Y.; Cabot, R.; Krap, C. P.; Lü, J.; Easun, T. L.; Bichoutskaia, E.; Lewis, W.; Blake, A. J.; Schröder, M., Chem. Eur. J. 2014, 20, 7317-7324. (23) Bent, H. A., Chem. Rev. 1968, 68, 587-648. (24) Zheng, B.; Bai, J.; Duan, J.; Wojtas, L.; Zaworotko, M. J., J. Am. Chem. Soc. 2011, 133, 748-751. (25) Lu, Z.; Xing, H.; Sun, R.; Bai, J.; Zheng, B.; Li, Y., Cryst. Growth Des. 2012, 12, 1081-1084. (26) Zheng, B.; Liu, H.; Wang, Z.; Yu, X.; Yi, P.; Bai, J., CrystEngComm 2013, 15, 3517-3520. (27) Duan, J.; Yang, Z.; Bai, J.; Zheng, B.; Li, Y.; Li, S., Chem. Commun. 2012, 48, 3058-3060. (28) Park, J.; Li, J.-R.; Chen, Y.-P.; Yu, J.; Yakovenko, A. A.; Wang, Z. U.; Sun, L.-B.; Balbuena, P. B.; Zhou, H.-C., Chem. Commun. 2012, 48, 9995-9997. (29) Luo, X.-Z.; Jia, X.-J.; Deng, J.-H.; Zhong, J.-L.; Liu, H.-J.; Wang, K.-J.; Zhong, D.-C., J. Am. Chem. Soc. 2013, 135, 1168411687. (30) Rajput, L.; Banerjee, R., Cryst. Growth Des. 2014, 14, 27292732. (31) Lin, R.-G.; Cao, G.-J.; Lin, J.-D.; Wang, Y.-L., New J. Chem. 2015, 39, 9075-9078. (32) Guillerm, V.; Kim, D.; Eubank, J. F.; Luebke, R.; Liu, X.; Adil, K.; Lah, M. S.; Eddaoudi, M., Chem. Soc. Rev. 2014, 43, 6141-6172. (33) Masoomi, M. Y.; Beheshti, S.; Morsali, A., J. Mater. Chem. A 2014, 2, 16863-16866. (34) Azhdari Tehrani, A.; Ghasempour, H.; Morsali, A.; Makhloufi, G.; Janiak, C., Cryst. Growth Des. 2015, 15, 55435547.

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Crystal Growth & Design

(35) Masoomi, M. Y.; Stylianou, K. C.; Morsali, A.; Retailleau, P.; Maspoch, D., Cryst. Growth Des. 2014, 14, 2092-2096. (36) Juanhuix, J.; Gil-Ortiz, F.; Cuni, G.; Colldelram, C.; Nicolas, J.; Lidon, J.; Boter, E.; Ruget, C.; Ferrer, S.; Benach, J., J. Synchr. Rad. 2014, 21, 679-689. (37) Kabsch, W., Acta Cryst. Sect. D 2010, 66, 125-132. (38) Leslie, A., Acta Cryst. Sect. D 2006, 62, 48-57. (39) Siemens SAINT, 4. Siemens Analytical X-ray Instruments Inc.: Madison, Wisconsin, USA., 1996. (40) Krause, L.; Herbst-Irmer, R.; Sheldrick, G. M.; Stalke, D., J. Appl. Crystallogr. 2015, 48, 3-10. (41) Sheldrick, G. M.; Dauter, Z.; Wilson, K. S.; Hope, H.; Sieker, L. C., Acta Cryst. Sect. D 1993, 49, 18-23. (42) Sheldrick, G., Acta Cryst. Sect. C 2015, 71, 3-8. (43) Farrugia, L., J. Appl. Crystallogr. 2012, 45, 849-854. (44) Spek, A. L., PLATON A Multipurpose Crystallographic Tool. Utrecht University: Utrecht (The Netherlands), 2001. (45) Addison, A. W.; Rao, T. N.; Reedijk, J.; van Rijn, J.; Verschoor, G. C., J. Chem. Soc., Dalton Trans. 1984, 1349-1356. (46) Spek, A. L., J. Appl. Crystallogr. 2003, 36, 7-13. (47) Blatov, V. A.; Shevchenko, A. P.; Proserpio, D. M., Cryst. Growth Des. 2014, 14, 3576-3586.

(48) Li, H.; Eddaoudi, M.; O'Keeffe, M.; Yaghi, O. M., Nature 1999, 402, 276-279. (49) Patel, H. A.; Hyun Je, S.; Park, J.; Chen, D. P.; Jung, Y.; Yavuz, C. T.; Coskun, A., Nature Commun. 2013, 4, 1357. (50) Ok, K. M.; Sung, J.; Hu, G.; Jacobs, R. M. J.; O'Hare, D., J. Am. Chem. Soc. 2008, 130, 3762-3763. (51) Jiang, J.-J.; Pan, M.; Liu, J.-M.; Wang, W.; Su, C.-Y., Inorg. Chem. 2010, 49, 10166-10173. (52) Maji, T. K.; Matsuda, R.; Kitagawa, S., Nat Mater 2007, 6, 142-148. (53) Liu, Y.; Her, J.-H.; Dailly, A.; Ramirez-Cuesta, A. J.; Neumann, D. A.; Brown, C. M., J. Am. Chem. Soc. 2008, 130, 11813-11818. (54) Thomas-Gipson, J.; Beobide, G.; Castillo, O.; Cepeda, J.; Luque, A.; Perez-Yanez, S.; Aguayo, A. T.; Roman, P., CrystEngComm 2011, 13, 3301-3305. (55) Horike, S.; Shimomura, S.; Kitagawa, S., Nature Chem. 2009, 1, 695-704. (56) Schneemann, A.; Bon, V.; Schwedler, I.; Senkovska, I.; Kaskel, S.; Fischer, R. A., Chem. Soc. Rev. 2014, 43, 6062-6096. (57) Férey, G.; Serre, C., Chem. Soc. Rev. 2009, 38, 1380-1399.

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For Table of Contents Use Only The influence of the amide groups in the CO2/N2 selectivity of a series of isoreticular, interpenetrated metal-organic frameworks. Vahid Safarifard, Sabina Rodríguez-Hermida, Vincent Guillerm, Inhar Imaz, Mina Bigdeli, Alireza A. Tehrani, Jordi Juanhuix, Ali Morsali,* Mirian E. Casco, Joaquín Silvestre-Albero, Enrique V. Ramos-Fernandez and Daniel Maspoch*

The accessibility of amide functional groups within MOF structures is crucial to obtain enhanced CO2 sorption and CO2/N2 selectivity.

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